Treatment of human tumor xenografts with monoclonal antibody 806 in combination with a prototypical epidermal growth factor receptor-specific antibody generates enhanced antitumor activity

被引:91
作者
Perera, RM
Narita, Y
Furnari, FB
Gan, HK
Murone, C
Ahikvist, M
Luwor, RB
Burgess, AW
Stockert, E
Jungbluth, AA
Old, LJ
Cavenee, WK
Scott, AM
Johns, TG
机构
[1] Austin Hosp, Oncogen Signalling Lab, Ludwig Inst Canc Res, Melbourne Branch,Tumor Targeting Program, Heidelberg, Vic 3084, Australia
[2] Univ Calif San Diego, Ludwig Inst Canc Res, San Diego Branch, La Jolla, CA 92093 USA
[3] Royal Melbourne Hosp, Epithelial Biochem Lab, Parkville, Vic 3050, Australia
[4] Ludwig Inst Canc Res, New York Branch, New York, NY USA
关键词
D O I
10.1158/1078-0432.CCR-04-2653
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Monoclonal antibody (mAb) 806 is a novel epidermal growth factor receptor (EGFR) antibody with significant antitumor activity that recognizes a mutant EGFR commonly expressed in glioma known as delta2-7 EGFR (de2-7 EGFR or EGFRvIII) and a subset of the wild-type (wt) EGFR found in cells that overexpress the receptor, We have used two human xenograft mouse models to examine the efficacy of mAb 806 in combination with mAb 528, a prototypical anti-EGFR antibody with similar specificity to cetuximab. Treatment of nude mice, bearing s.c. or i.c. tumor human xenografts expressing the wt or de2-7 EGFR, with mAbs 806 and 528 in combination resulted in additive and in some cases synergistic, antitumor activity. Interestingly, mAb 528 was also effective against xenografts expressing the ligand independent de2-7 EGFR when used as a single agent, showing that its antitumor activity is not merely mediated through inhibition of ligand binding. When used as single agents, neither mAbs 806 or 528 induced down-regulation of the de2-7 EGFR either in vitro or in vivo. In contrast, the combination of antibodies produced a rapid and dramatic decrease in the total cell surface de2-7 EGFR both in vitro and in xenografts. Consistent with this decrease in total cell surface de2-7 EGFR, we observed up-regulation of the cell cycle inhibitor p27(KIP1) and a decrease in tumor cell proliferation as measured by Ki-67 immunostaining when the antibodies were used in combination in vivo. Thus, mAb 806 can synergize with other EGFR-specific antibodies thereby providing a rationale for its translation into the clinic.
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页码:6390 / 6399
页数:10
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